HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278503Generated: October 31, 2026
4,5,6-Trichloro-2-methylpyrimidine → HCID 15003621, compound
https://huagongshe.com/reaction/2278503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,5,6-Trichloro-2-methylpyrimidine | HCID 231054 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15003621 | HCID 15003621 | 96.8% |
Reaction Steps
1.37 g of sodium methoxide are added to a solution of 5 g of 2-methyl-4,5,6-trichloropyrimidine in 41 ml of THF cooled to 5° C. in an ice bath. The ice bath is removed. The suspension is stirred at ambient temperature for 18 hours. The reaction medium is cooled to 5° C. in an ice bath. 20 ml of water and 100 ml of ethyl acetate are added. After settling out, the organic phase is dried over magnesium sulfate, filtered, and concentrated under reduced pressure so as to give 4.73 g of 4,5-dichloro-6-methoxy-2-methylpyrimidine in the form of a colorless oil which crystallizes, the characteristics of which are the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133168B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-9879af4a3e9f413faeb4d7b3182b496b |
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| Source note | uspto-grants-2015_09 |
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